External biological activity determination method for human insulin and analog or conjugate
A technology for human insulin, analogs, applied in the measurement of color/spectral properties, analysis by chemical reaction of materials, material analysis by observing the effect on chemical indicators, etc., can solve fragile, ineffective counting and Repeatability, etc.
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Embodiment 1
[0021] Example 1 Comparison of Three Determination Methods of Recombinant Human Regular Insulin In Vitro Biological Potency Determination
[0022] Using 3T3-L1 preadipocytes (purchased from Shanghai Cell Bank, Chinese Academy of Sciences) and male rat preadipocytes (purchased from male rats from the Animal Institute of Daping Hospital, Third Military Medical University) to measure the activity of recombinant human insulin, recombinant human Ordinary insulin standard (from China National Institutes for Food and Drug Control, each labeled content is 20mg / bottle 28.3IU / mg).
[0023] Rat preadipocyte GOD-POD method
[0024] (1) Take 90g-120g male rats fed with common food, decapitate them after ether anesthesia, soak them in 75% alcohol for complete disinfection, and cut out the abdominal groove, epididymis, and fat pads around the kidneys under aseptic conditions and put them in a petri dish In PBS, use surgical scissors to remove blood vessels and lymph nodes as much as possibl...
Embodiment 2
[0048] Example 2 Glucose oxidase method (GOD-POD method) and 3H-glucose radiation assay experiments in the determination of the biological potency of recombinant human insulin standard and insulin detemir in rat preadipocytes
[0049] The method in Example 1 was used to induce preadipocytes in male rats, and after the cells were induced into 80% adipocytes, they were used for the following experiments.
[0050] Glucose oxidase method (POD method): Add 1.0mg / ml glucose and 0.8μCi / well 3H-Glucose to DMEM glucose-free medium as cell maintenance solution. Add 180 μl of cell maintenance solution to each well after discarding the cell fluid from the adipocytes, and dilute the recombinant human insulin standard (from China National Institutes for Food and Drug Control, 20 mg / tube, 28.3 IU / mg per tube) to 5 μg / ml; Insulin tephra (from Novo Nordisk NovoPing 300 units / 3ml / bottle) was diluted to 20 μg / ml and started to be diluted 3 times, making eight dilutions, adding 20 μl of sample to...
Embodiment 3
[0056] Example 3 Determination of rapid-acting insulin, long-acting insulin and modified conjugate (PEG-Lispro) in vitro activity of rat preadipocytes
[0057] Utilize the method for inducing rat preadipocytes in Example 1 to measure insulin aspart (derived from Novo Nordisk Novo Sharp 300 units / 3ml / branch), insulin lispro (derived from Lilly Humalog 300 units) / 3ml / bottle), ordinary human insulin (from China Food and Drug Control Institute), insulin glargine (from Sanofi-Aventis Lantus 300 units / 3ml / bottle), insulin detemir (from The in vitro biological activity of Novo Nordisk Novoping 300 units / 3ml / branch) and PEG-Lispro (made by the company according to the patent EP2476430A1), the half-effective response dose (EC50) after 5 repeated tests, the results are as follows Figure 5 .
[0058] After 5 repeated determinations of the recombinant human insulin potency standard product, the half-effective dose EC50 average value is 17.754ng / ml. Based on the potency standard product...
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